Kearns R J, Hinrichs D J
Infect Immun. 1977 Jun;16(3):923-7. doi: 10.1128/iai.16.3.923-927.1977.
In the mouse system, acquired resistance to Listeria monocytogenes can only be demonstrated after immunization with viable microorganisms. A successful state of immunity cannot be elicited with formalin-killed organisms or bacterial cell-derived products. Viable, serologically cross-reactive organisms (not mouse pathogenic) do not induce a state of immunity as measured by acquired resistance. The duration of immunity, once established, is dose independent, and the absolute interval of its existence is not extended by secondary challenge with large numbers of viable organisms. The decline of immunity in actively immunized animals is not altered by antigenic challenge with formalin-killed cells or cell products. This indicates that the cellular requirements for the development of host resistance are similar for induction as well as maintenance. In vitro measurements of cellular immunity by migration inhibition indicate that formalin-killed organisms as well as cell products were recognized by actively sensitized lymphocytes obtained from immune animals.
在小鼠系统中,只有在用活的微生物免疫后,才能证明对单核细胞增生李斯特菌产生了获得性抗性。用福尔马林灭活的生物体或细菌细胞衍生产品无法引发成功的免疫状态。活的、血清学交叉反应性生物体(非小鼠致病性)不会诱导出通过获得性抗性衡量的免疫状态。一旦建立,免疫持续时间与剂量无关,并且其存在的绝对间隔不会因用大量活生物体进行二次攻击而延长。主动免疫动物中免疫力的下降不会因用福尔马林灭活的细胞或细胞产品进行抗原攻击而改变。这表明宿主抗性发展所需的细胞条件在诱导和维持方面是相似的。通过迁移抑制对细胞免疫进行的体外测量表明,福尔马林灭活的生物体以及细胞产品能够被从免疫动物获得的主动致敏淋巴细胞识别。